Package 82804-120-90

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 82804-120-90
Digits Only 8280412090
Product NDC 82804-120
Product ID 82804-120_c6606db5-3937-4e90-9870-3cbfa4ec909e
Description

90 TABLET in 1 BOTTLE (82804-120-90)

Marketing

Marketing Status
Marketed Since 2024-07-08
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Nebivolol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c6606db5-3937-4e90-9870-3cbfa4ec909e", "openfda": {"upc": ["0382804120901"], "unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["c6606db5-3937-4e90-9870-3cbfa4ec909e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-120-90)", "package_ndc": "82804-120-90", "marketing_start_date": "20240708"}], "brand_name": "Nebivolol", "product_id": "82804-120_c6606db5-3937-4e90-9870-3cbfa4ec909e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82804-120", "generic_name": "Nebivolol", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203825", "marketing_category": "ANDA", "marketing_start_date": "20210917", "listing_expiration_date": "20261231"}